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Hedgehog Signaling in the Maintenance of Cancer Stem Cells

Cancer stem cells (CSCs) represent a rare population of cells with the capacity to self-renew and give rise to heterogeneous cell lineages within a tumour. Whilst the mechanisms underlying the regulation of CSCs are poorly defined, key developmental signaling pathways required for normal stem and pr...

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Detalles Bibliográficos
Autores principales: Cochrane, Catherine R., Szczepny, Anette, Watkins, D. Neil, Cain, Jason E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586784/
https://www.ncbi.nlm.nih.gov/pubmed/26270676
http://dx.doi.org/10.3390/cancers7030851
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author Cochrane, Catherine R.
Szczepny, Anette
Watkins, D. Neil
Cain, Jason E.
author_facet Cochrane, Catherine R.
Szczepny, Anette
Watkins, D. Neil
Cain, Jason E.
author_sort Cochrane, Catherine R.
collection PubMed
description Cancer stem cells (CSCs) represent a rare population of cells with the capacity to self-renew and give rise to heterogeneous cell lineages within a tumour. Whilst the mechanisms underlying the regulation of CSCs are poorly defined, key developmental signaling pathways required for normal stem and progenitor functions have been strongly implicated. Hedgehog (Hh) signaling is an evolutionarily-conserved pathway essential for self-renewal and cell fate determination. Aberrant Hh signaling is associated with the development and progression of various types of cancer and is implicated in multiple aspects of tumourigenesis, including the maintenance of CSCs. Here, we discuss the mounting evidence suggestive of Hh-driven CSCs in the context of haematological malignancies and solid tumours and the novel strategies that hold the potential to block many aspects of the transformation attributed to the CSC phenotype, including chemotherapeutic resistance, relapse and metastasis.
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spelling pubmed-45867842015-10-06 Hedgehog Signaling in the Maintenance of Cancer Stem Cells Cochrane, Catherine R. Szczepny, Anette Watkins, D. Neil Cain, Jason E. Cancers (Basel) Review Cancer stem cells (CSCs) represent a rare population of cells with the capacity to self-renew and give rise to heterogeneous cell lineages within a tumour. Whilst the mechanisms underlying the regulation of CSCs are poorly defined, key developmental signaling pathways required for normal stem and progenitor functions have been strongly implicated. Hedgehog (Hh) signaling is an evolutionarily-conserved pathway essential for self-renewal and cell fate determination. Aberrant Hh signaling is associated with the development and progression of various types of cancer and is implicated in multiple aspects of tumourigenesis, including the maintenance of CSCs. Here, we discuss the mounting evidence suggestive of Hh-driven CSCs in the context of haematological malignancies and solid tumours and the novel strategies that hold the potential to block many aspects of the transformation attributed to the CSC phenotype, including chemotherapeutic resistance, relapse and metastasis. MDPI 2015-08-11 /pmc/articles/PMC4586784/ /pubmed/26270676 http://dx.doi.org/10.3390/cancers7030851 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Cochrane, Catherine R.
Szczepny, Anette
Watkins, D. Neil
Cain, Jason E.
Hedgehog Signaling in the Maintenance of Cancer Stem Cells
title Hedgehog Signaling in the Maintenance of Cancer Stem Cells
title_full Hedgehog Signaling in the Maintenance of Cancer Stem Cells
title_fullStr Hedgehog Signaling in the Maintenance of Cancer Stem Cells
title_full_unstemmed Hedgehog Signaling in the Maintenance of Cancer Stem Cells
title_short Hedgehog Signaling in the Maintenance of Cancer Stem Cells
title_sort hedgehog signaling in the maintenance of cancer stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586784/
https://www.ncbi.nlm.nih.gov/pubmed/26270676
http://dx.doi.org/10.3390/cancers7030851
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